Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5226987A>T	CA125235	HBB	c.35T>A (p.Val12Asp) n.86T>A	ClinVar dbSNP
11	g.5226987A=	CA1949570832	HBB	c.35T= (p.Val12=) n.86T=	dbSNP

Number of alleles fetched